| Tag | Content |
|---|
EnhancerAtlas ID | HS138-44534 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chrX:16761960-16762700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chrX:16762289-16762299 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chrX:16762289-16762299 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chrX:16762289-16762299 | ATTTTCCATT | + | 6.02 | | RUNX1 | MA0002.2 | chrX:16762209-16762220 | AAACCACAAAC | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH0XI016743 | chrX | 16761745 | 16762994 |
|
Enhancer Sequence | ACTGTAAGCA GAGTGTTCTC CAGCGTTTCC TCATGGCCTC CATTATGTGC TCAGTATCAG 60
CACATAATGA TGGAAGGGGC CAAAAGGGTC TCTATCTGTT CATAAAAGCA GGCCCCGCAG 120
CCCTTTGGCA GCTCCCCTGG TCAGGGCACT CTGGAATCAA AACCAAGGTC TGACTTGGCA 180
GGAAATACAG GGTAGAGGTG AAATGTGCTT TTCTATCCCA GTTACAAGGT AGAACACATT 240
TCCCTACAGA AACCACAAAC ATGCTGCATC ACCCTGAATC ACATTCTGGT CTCTGAGGCT 300
CATCGGGATC TTTTTTCCAA GCTGACTGCA TTTTCCATTC AGGCTCTGCC CTCCAGTGGC 360
AGTGTTCCTG CTCTCTTTGC TAAGGCTTTT CCTCCAACAG CTCTTCTGGG CTCCACAAAT 420
CCCAGCTTGT CCTGTAGGCT CCAGTGCATG CATGATGCAT TCTGGAAGCC TGCCTTGGTG 480
GTGCGGCCAA CAGGGGCCAC CTTCCCCGCT GCTGCTTCCC TTGGGTGTTC TGTCTCAAGC 540
TCTTCCGTGC CTTCTCCAGT CCAGTCCCTT GTATTGAAGC TGTCGCATGT TTGGAGTCAG 600
CGTTCCTTCT TATTCTGTCA TTGTTCCCTT TCTCTTAACC TTGTCATATG GGTGCAGTAT 660
CTTACTGTTC CCTGAGTACG TTAGTTACAG TTCTCTCAAA AGACTCCTTT TTCAGCTGGG 720
TGCGGTGGCC AATGCCTGTA 740
|
